NDC 57237-142
Amlodipine and Benazepril Hydrochloride 10 mg / 2.5 mg capsule
On the label: Rising Pharma Holdings, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Amlodipine and Benazeprilat: every company that makes it
- Form
- capsule, oral
- Strength
- 10 mg / 2.5 mg
- Approval
- ANDA ANDA202239
- On the market since
- Sep 5, 2012
- Package NDCs
57237-142-0157237-142-05- Official label
- DailyMed (National Library of Medicine), updated Aug 31, 2024
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